FAM63A 抗体 (Alexa Fluor 594)
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- 抗原 See all FAM63A 抗体
- FAM63A (Family with Sequence Similarity 63, Member A (FAM63A))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This FAM63A antibody is conjugated to Alexa Fluor 594
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应用范围
- Western Blotting (WB)
- 交叉反应
- 人, 小鼠
- 预测反应
- Rat,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM63A
- 亚型
- IgG
- Top Product
- Discover our top product FAM63A Primary Antibody
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anti-Family with Sequence Similarity 63, Member A (FAM63A) antibody
FAM63A 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 63, Member A (FAM63A) (C-Term) antibodyFAM63A 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 猴 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 1:50-200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- FAM63A (Family with Sequence Similarity 63, Member A (FAM63A))
- 别名
- FAM63A (FAM63A 产品)
- 别名
- RP11-316M1.5 antibody, 1810005H09Rik antibody, 4930504E06Rik antibody, AA562754 antibody, AA960384 antibody, AW561904 antibody, cI-40 antibody, mKIAA1390 antibody, ni antibody, si:ch211-210h11.5 antibody, MINDY lysine 48 deubiquitinase 1 antibody, MINDY1 antibody, Mindy1 antibody, mindy1 antibody
- 背景
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Synonyms: FA63A_HUMAN, FAM 63A, FAM63A, Family with sequence similarity 63 member A, FLJ11280, FLJ43504, Hypothetical protein LOC55793, KIAA1390, Protein FAM63A.
Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM63A gene product has been provisionally designated FAM63A pending further characterization.
- 基因ID
- 55793
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